IMO Practice Test — Biomolecules
13 Questions • 15 min • Olympiad level
15:00
Question 1 of 13
A sugar gives a positive Tollens' test but does not react with Schiff's reagent and shows mutarotation. The sugar is most likely:
sucrose
glucose
a non-sugar polysaccharide
an amino acid
Explanation: Glucose reduces Tollens' (open chain available) yet, being almost entirely cyclic, gives a negative Schiff's test and shows mutarotation.
Question 2 of 13
Equimolar hydrolysis of sucrose changes rotation from +66.5° to about −20° mainly because:
glucose is strongly laevorotatory
fructose is strongly laevorotatory
both products are dextrorotatory
water rotates light
Explanation: Fructose (−92°) outweighs glucose (+52.5°), making the invert-sugar mixture net laevorotatory.
Question 3 of 13
Two DNA samples X and Y melt (separate) at 75°C and 90°C respectively. Compared with X, sample Y is richer in:
A=T pairs
G≡C pairs
uracil
ribose
Explanation: G≡C pairs have three H-bonds versus two in A=T, so a higher G≡C content needs a higher melting temperature.
Question 4 of 13
At a pH equal to its isoelectric point, an amino acid placed in an electric field will:
move to the cathode
move to the anode
not migrate
decompose
Explanation: At the pI the net charge is zero (pure zwitterion), so there is no migration toward either electrode.
Question 5 of 13
Glycine has no D/L isomers because:
it is the smallest amino acid
its α-carbon is not a chiral centre
it is fat-soluble
it lacks a –COOH group
Explanation: In glycine the α-carbon carries two H atoms, so it has no four different groups and is not chiral — hence no optical isomers.
Question 6 of 13
A single DNA strand reads 5′-ATGC-3′. The complementary strand (5′→3′) is:
5′-TACG-3′
5′-GCAT-3′
5′-CGTA-3′
5′-ATGC-3′
Explanation: Pairing A–T, T–A, G–C, C–G gives the antiparallel complement, which read 5′→3′ is GCAT.
Question 7 of 13
Boiling does not change the molar mass measured for the peptide chain of a denatured protein because denaturation:
hydrolyses peptide bonds
leaves the primary structure intact
removes amino acids
adds water across each bond
Explanation: Denaturation breaks only the weak forces of the 2°/3° structure; the covalently bonded primary chain (and its mass) is unchanged.
Question 8 of 13
A patient stores a vitamin in the liver and develops toxicity on overdose. This vitamin is most likely:
vitamin C
vitamin B1
vitamin A
vitamin B12
Explanation: Fat-soluble vitamins (A, D, E, K) are stored in the liver/fat and can reach toxic levels; water-soluble ones are excreted.
Question 9 of 13
Cellulose and starch are both glucose polymers, yet only starch is digestible by humans. The key reason is the:
number of glucose units
presence of nitrogen
molar mass difference
type of glycosidic linkage (α vs β)
Explanation: Human amylase hydrolyses α-1,4 links (starch) but not β-1,4 links (cellulose).
Question 10 of 13
In protein synthesis the correct flow of genetic information is:
protein → mRNA → DNA
DNA → mRNA → protein
mRNA → DNA → protein
tRNA → DNA → mRNA
Explanation: DNA is transcribed to mRNA, which is translated on the ribosome to protein — the central dogma.
Question 11 of 13
Fructose forms a five-membered ring whereas glucose forms a six-membered ring because in fructose the ring closes between the:
C1 aldehyde and C5–OH
C2 keto group and C5–OH
C1 and C2
C6 and C1
Explanation: The C2 keto carbon of fructose reacts with the C5–OH to give a five-membered furanose ring; glucose's C1–CHO with C5–OH gives a six-membered pyranose ring.
Question 12 of 13
Which statement about Chargaff's rule for double-stranded DNA is correct?
A + G = C + T (purines = pyrimidines)
A = G and T = C
A + T = 0
all four bases are equal
Explanation: Because A pairs with T and G with C, the total purines (A+G) equal the total pyrimidines (C+T), and A=T, G=C individually.
Question 13 of 13
Maltose is reducing while sucrose is not. This is best explained by maltose having:
a free anomeric –OH (potential aldehyde)
an extra phosphate
a peptide bond
no glycosidic bond
Explanation: Maltose keeps one free anomeric carbon that can open to an aldehyde; sucrose locks both anomeric carbons, so it is non-reducing.